Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data von Glessner, Joseph T, Bick, Alexander G, Ito, Kaoru, Homsy, Jason G, Rodriguez-Murillo, Laura, Fromer, Menachem, Mazaika, Erica, Vardarajan, Badri, Italia, Michael, Leipzig, Jeremy, DePalma, Steven R, Golhar, Ryan, Sanders, Stephan J, Yamrom, Boris, Ronemus, Michael, Iossifov, Ivan, Willsey, A Jeremy, State, Matthew W, Kaltman, Jonathan R, White, Peter S, Shen, Yufeng, Warburton, Dorothy, Brueckner, Martina, Seidman, Christine, Goldmuntz, Elizabeth, Gelb, Bruce D, Lifton, Richard, Seidman, Jonathan, Hakonarson, Hakon, Chung, Wendy K

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The Genetic Architecture of Schizophrenia: New Mutations and Emerging Paradigms von Rodriguez-Murillo, Laura, Gogos, Joseph A, Karayiorgou, Maria

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Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans von Xu, Bin, Woodroffe, Abigail, Rodriguez-Murillo, Laura, Roos, J. Louw, van Rensburg, Elizabeth J, Abecasis, Gonçalo R, Gogos, Joseph A, Karayiorgou, Maria

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COL1A1 association and otosclerosis: A meta-analysis von Schrauwen, Isabelle, Khalfallah, Ayda, Ealy, Megan, Fransen, Erik, Claes, Charlotte, Huber, Alex, Murillo, Laura Rodriguez, Masmoudi, Saber, Smith, Richard J.H., Van Camp, Guy

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Multipoint lods provide reliable linkage evidence despite unknown limiting distribution: type I error probabilities decrease with sample size for multipoint lods and mods von Hodge, Susan E., Rodriguez-Murillo, Laura, Strug, Lisa J., Greenberg, David A.

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Novel loci interacting epistatically with bone morphogenetic protein receptor 2 cause familial pulmonary arterial hypertension von Rodriguez-Murillo, Laura, PhD, Subaran, Ryan, PhD, Stewart, William C.L., PhD, Pramanik, Sreemanta, PhD, Marathe, Sudhir, PhD, Barst, Robyn J., MD, Chung, Wendy K., MD, Greenberg, David A., PhD

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Genetic association analysis: a primer on how it works, its strengths and its weaknesses von Rodriguez-Murillo, Laura, Greenberg, David A.

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A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure von Granot-Hershkovitz, Einat, Karasik, David, Friedlander, Yechiel, Rodriguez-Murillo, Laura, Dorajoo, Rajkumar, Liu, Jianjun, Sewda, Anshuman, Peter, Inga, Carmi, Shai, Hochner, Hagit

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C9ORF72 repeat expansions not detected in a group of patients with schizophrenia von Huey, Edward D, Nagy, Peter L, Rodriguez-Murillo, Laura, Manoochehri, Masood, Goldman, Jill, Lieberman, Jeffrey, Karayiorgou, Maria, Mayeux, Richard

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Fine Mapping on Chromosome 13q32-34 and Brain Expression Analysis Implicates MYO16 in Schizophrenia von RODRIGUEZ-MURILLO, Laura, BIN XU, ROOS, J. Louw, ABECASIS, Gonçalo R, GOGOS, Joseph A, KARAYIORGOU, Maria

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A genetic signature for complex psychiatric diseases von Rodríguez-Murillo, Laura, Lieberman, Jeffrey A

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Increased Frequency of De Novo Copy Number Variations in Congenital Heart Disease by Integrative Analysis of SNP Array and Exome Sequence Data von Glessner, Joseph T., Bick, Alexander G., Ito, Kaoru, Homsy, Jason, Rodriguez-Murillo, Laura, Fromer, Menachem, Mazaika, Erica, Vardarajan, Badri, Italia, Michael, Leipzig, Jeremy, DePalma, Steven R., Golhar, Ryan, Sanders, Stephan J., Yamrom, Boris, Ronemus, Michael, Iossifov, Ivan, Willsey, A. Jeremy, State, Matthew W., Kaltman, Jonathan R., White, Peter S., Shen, Yufeng, Warburton, Dorothy, Brueckner, Martina, Seidman, Christine, Goldmuntz, Elizabeth, Gelb, Bruce D., Lifton, Richard, Seidman, Jonathan, Hakonarson, Hakon, Chung, Wendy K.

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Genotype von Rodriguez-Murillo, Laura, Salem, Rany M.

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Recessive Inheritance von Rodriguez-Murillo, Laura, Salem, Rany M.

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Homozygous von Rodriguez-Murillo, Laura, Salem, Rany M.

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Human Genome Project von Salem, Rany M., Rodriguez-Murillo, Laura

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Copy Number Variant (CNV) von Salem, Rany M., Rodriguez-Murillo, Laura

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Insertion/Deletion Polymorphism von Rodriguez-Murillo, Laura, Salem, Rany M.

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Heterozygous von Rodriguez-Murillo, Laura, Salem, Rany M.

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Chromosomes von Salem, Rany M., Rodriguez-Murillo, Laura

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